Difference between revisions of "Part:BBa J100341:Experience"
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Here is the figure for v2 of actClone PM, 2017. | Here is the figure for v2 of actClone PM, 2017. | ||
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[[File:PMrepClone2_real.png|500px]] | [[File:PMrepClone2_real.png|500px]] | ||
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− | + | We measured the average cell fluorescence to cell density ratio for E. coli cells grown in the following conditions: one experimental group transformed with the J100341 promoter (X1), two wild-type groups (TWT and JWT) and another scrambled wildtype promoter (SWT). Each of those groups were divided and placed into separate liquid cultures – one lacking ATC and the other with 3 uL of 0.2ug/mL ATC. A positive control group containing the plasmid with the J04450 promoter and a negative control group (J100205) which contained untransformed cells were also grown in liquid culture. The cells were run in triplicates. Error bars represent standard error. | |
===Applications of BBa_J100341=== | ===Applications of BBa_J100341=== | ||
Latest revision as of 19:24, 16 November 2017
Here is the figure for v2 of actClone PM, 2017.
We measured the average cell fluorescence to cell density ratio for E. coli cells grown in the following conditions: one experimental group transformed with the J100341 promoter (X1), two wild-type groups (TWT and JWT) and another scrambled wildtype promoter (SWT). Each of those groups were divided and placed into separate liquid cultures – one lacking ATC and the other with 3 uL of 0.2ug/mL ATC. A positive control group containing the plasmid with the J04450 promoter and a negative control group (J100205) which contained untransformed cells were also grown in liquid culture. The cells were run in triplicates. Error bars represent standard error.
Applications of BBa_J100341
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